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FDA 510(k)

EXPANSION OF THE CORDIS PTA DILATATION CATHETER

K-Number: K894899 · 1990-01-26

ApplicantCordis Corp.
Decision Date1990-01-26
Product CodeLIT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

EXPANSION OF THE CORDIS PTA DILATATION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1990-01-26 under 510(k) number K894899. The device is classified under product code LIT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXPANSION OF THE CORDIS PTA DILATATION CATHETER?

EXPANSION OF THE CORDIS PTA DILATATION CATHETER is a medical device that received FDA 510(k) clearance on 1990-01-26. The listed applicant is Cordis Corp.. The 510(k) number is K894899.

When did EXPANSION OF THE CORDIS PTA DILATATION CATHETER receive FDA 510(k) clearance?

EXPANSION OF THE CORDIS PTA DILATATION CATHETER received FDA 510(k) clearance on 1990-01-26, under 510(k) number K894899.

Who is the listed applicant for EXPANSION OF THE CORDIS PTA DILATATION CATHETER?

The FDA 510(k) record lists Cordis Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EXPANSION OF THE CORDIS PTA DILATATION CATHETER?

The FDA product code for EXPANSION OF THE CORDIS PTA DILATATION CATHETER is LIT.

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Other records listing Cordis Corp. as applicant

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Related Devices (Code: LIT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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